2013
DOI: 10.1016/j.tsf.2012.11.081
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In-situ phase formation study of copper indium diselenide absorber layers from CuIn nanoparticles and evaporated selenium

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Cited by 9 publications
(9 citation statements)
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“…6 shows the development of the surface structure during annealing. All samples show a porous layer and a grain size of about 100 nm which is in the range of Cu-In nanoparticles reported in earlier work [18,21]. The major difference can be found between the as deposited sample and the annealed samples.…”
Section: Ex-situ Phase Characterisation (X = 00)supporting
confidence: 50%
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“…6 shows the development of the surface structure during annealing. All samples show a porous layer and a grain size of about 100 nm which is in the range of Cu-In nanoparticles reported in earlier work [18,21]. The major difference can be found between the as deposited sample and the annealed samples.…”
Section: Ex-situ Phase Characterisation (X = 00)supporting
confidence: 50%
“…Metallic Cu-In nanoparticles (see e.g. [18]) and elemental selenium nanoparticles, comparable to the one used by Dhage et al [19] containing Cu-In-Ga and Se nanoparticles. Furthermore Cu-Ga powder was prepared and dispersed in an ink.…”
Section: Introductionmentioning
confidence: 87%
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“…In situ XRD is a valuable tool to investigate the formation processes of thin film solar cell absorber layers. In the past, it has been used to analyze the selenizaton and sulfo‐selenizaton of Cu–In–Ga precursors layers for Cu(In,Ga)(S,Se) 2 solar cells , the sulfo‐selenization of Cu–In precursor layers for CuIn(S,Se) 2 solar cells , and both the sulfurization and selenization of Cu–Zn–Sn precursor layers for CZTS and CZTSe solar cells . Recently, Rodriguez‐Alvarez et al investigated the growth of CuInSe 2 and CuGaSe 2 by a co‐evaporation process with energy‐dispersive X‐ray diffraction (EDXRD), but a detailed study of CZTSe or CZTS film growth with thermal co‐evaporation has not been performed so far.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, diffusion processes and chemical reactions are hindered and a complete transformation of the precursor was prevented. This could be overcome by an excess of Se NP, as In 2 O 3 has been transformed back to selenide in earlier work [23,24], which can continue the reaction to CISe and consume the possibly left-over Cu 2−x Se. The morphology of the final film needs even more optimization compared with route I in terms of surface coverage and porosity.…”
Section: Discussionmentioning
confidence: 99%